Canonical Allele Identifier: CA363577310

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1781476565
• gnomAD v3: 6-32642199-T-G
• gnomAD v4: 6-32642199-T-G
• MyVariant Identifiers: chr6:g.32609976T>G (hg19) ; chr6:g.32642199T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642199T>G , CM000668.2:g.32642199T>G	GRCh38
NC_000006.11:g.32609976T>G , CM000668.1:g.32609976T>G	GRCh37
NC_000006.10:g.32717954T>G	NCBI36
NG_032876.1:g.9794T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343139.11:c.559T>G MANE Select	ENSP00000339398.5:p.Tyr187Asp
ENST00000343139.9:c.559T>G	ENSP00000339398.5:p.Tyr187Asp
ENST00000374949.2:c.559T>G	ENSP00000364087.2:p.Tyr187Asp
ENST00000395363.5:c.559T>G	ENSP00000378767.1:p.Tyr187Asp
ENST00000460633.1:n.587T>G
ENST00000482745.5:c.*1391T>G	ENSP00000436546.1:n.*1391T>G
ENST00000496318.5:c.559T>G	ENSP00000437302.1:p.Tyr187Asp
NM_002122.3:c.559T>G	NP_002113.2:p.Tyr187Asp
XM_006715079.2:c.559T>G	XP_006715142.1:p.Tyr187Asp
XM_006715079.4:c.559T>G	XP_006715142.1:p.Tyr187Asp
XR_001744085.1:n.86+389A>C
NM_002122.5:c.559T>G MANE Select	NP_002113.2:p.Tyr187Asp